Canonical Allele Identifier: CA1182717184
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098502A= , CM000663.2:g.97098502A= GRCh38
NC_000001.10:g.97564058A= , CM000663.1:g.97564058A= GRCh37
NC_000001.9:g.97336646A= NCBI36
NG_008807.2:g.827558T= , LRG_722:g.827558T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2753T= (DPYD) MANE Select ENSP00000359211.3:p.Ile918=
ENST00000370192.7:c.2753T= (DPYD) ENSP00000359211.3:p.Ile918=
NM_000110.3:c.2753T= , LRG_722t1:c.2753T= (DPYD) NP_000101.2:p.Ile918=
NR_046590.1:n.64+2516A= (DPYD-AS1)
XM_005270562.3:c.2537T= (DPYD) XP_005270619.2:p.Ile846=
XM_017000507.1:c.2642T= (DPYD) XP_016855996.1:p.Ile881=
XM_017000508.2:c.2258T= (DPYD) XP_016855997.1:p.Ile753=
XM_017000509.2:c.2258T= (DPYD) XP_016855998.1:p.Ile753=
XM_017000510.1:c.2258T= (DPYD) XP_016855999.1:p.Ile753=
NM_000110.4:c.2753T= (DPYD) MANE Select NP_000101.2:p.Ile918=